Peyrot, W. J., Van der Auwera, S., Milaneschi, Y., Dolan, C. V., Madden, P. A. F., Sullivan, P. F., Strohmaier, J., Ripke, S., Rietschel, M., Nivard, M. G., Mullins, N., Montgomery, G. W., Henders, A. K., Heat, A. C., Fisher, H. L., Dunn, E. C., Byrne, E. M., Air, T. A., Baune, B. T. ... Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium (2018).
Does Childhood Trauma Moderate Polygenic Risk for Depression? A Meta-analysis of 5765 Subjects From the Psychiatric Genomics Consortium.
Biological Psychiatry,
84(2), 138-147.
https://doi.org/10.1016/j.biopsych.2017.09.009
Pettersson, E., Lichtenstein, P., Larsson, H., Song, J., Attention Deficit/Hyperactivity Disorder Working Group of the iPSYCH-Broad-PGC Consortium, Autism Spectrum Disorder Working Group of the iPSYCH-Broad-PGC Consortium, Bipolar Disorder Working Group of the PGC, Eating Disorder Working Group of the PGC, Major Depressive Disorder Working Group of the PGC, Obsessive Compulsive Disorders and Tourette Syndrome Working Group of the PGC, Schizophrenia CLOZUK, Substance Use Disorder Working Group of the PGC , Agrawal, A.
, Borglum, A. D., Bulik, C. M., Daly, M. J., Davis, L. K.
, Demontis, D., Edenberg, H. J.
, Grove, J., Gelernter, J., Neale, B. M., Pardiñas, A. F., Stahl, E., Walters, J. T. R., Walters, R. ... Polderman, T. J. C. (2019).
Genetic influences on eight psychiatric disorders based on family data of 4 408 646 full and half-siblings, and genetic data of 333 748 cases and controls.
Psychological Medicine,
49(7), 1166-1173.
https://doi.org/10.1017/S0033291718002039
Pettersson, E., Lichtenstein, P., Larsson, H., Song, J., Attention Deficit/Hyperactivity Disorder Working Group of the iPSYCH-Broad-PGC Consortium, Autism Spectrum Disorder Working Group of the iPSYCH-Broad-PGC Consortium, Bipolar Disorder Working Group of the PGC, Eating Disorder Working Group of the PGC, Major Depressive Disorder Working Group of the PGC, Obsessive Compulsive Disorders and Tourette Syndrome Working Group of the PGC, Schizophrenia CLOZUK, Substance Use Disorder Working Group of the PGC , Agrawal, A.
, Børglum, A. D., Bulik, C. M., Daly, M. J., Davis, L. K.
, Demontis, D., Edenberg, H. J.
, Grove, J., Gelernter, J., Neale, B. M., Pardiñas, A. F., Stahl, E., Walters, J. T. R., Walters, R. ... Polderman, T. J. C. (2019).
Genetic influences on eight psychiatric disorders based on family data of 4 408 646 full and half-siblings, and genetic data of 333 748 cases and controls - CORRIGENDUM.
Psychological Medicine,
49(2), 351.
https://doi.org/10.1017/S0033291718002945
Petersen, M., Andersen, J. T., Hjelvang, B. R., Broedbaek, K., Afzal, S.
, Nyegaard, M., Børglum, A. D., Stender, S., Køber, L. V., Torp-Pedersen, C. T. & Poulsen, H. E. (2011).
Association of beta-adrenergic receptor polymorphisms and mortality in carvedilol-treated chronic heart-failure patients.
British Journal of Clinical Pharmacology,
71(4), 556-565.
https://doi.org/10.1111/j.1365-2125.2010.03868.x
Petersen, M., Andersen, J., Jimenez-Solem, E., Broedbaek, K.
, Afzal, S., Nyegaard, M., Børglum, A. D., Stender, S., Torp-Pedersen, C. T., Køber, L. V. & Poulsen, H. (2012).
Effect of specific ADRB1/ADRB2/AGT genotype combinations on the association between survival and carvedilol treatment in chronic heart failure: a substudy of the ECHOS trial.
Pharmacogenetics and Genomics,
22(10), 709-715.
https://doi.org/10.1097/FPC.0b013e3283540286
Pers, T. H., Hansen, N. T., Hansen, K. L., Koefoed, P., Dworzynski, P., Miller, M. L.
, Zacharov, T. F., Mellerup, E. T., Dam, H. F., Andreassen, O. A., Djurovic, S., Melle, I.
, Børglum, A. D., Werge, T., Purcell, S., Ferreira, M. A., Kouskoumvekaki, I., Workman, C., Hansen, T. ... Brunak, S. (2011).
Meta-analysis of heterogeneous data sources for genome-scale identification of risk genes in complex phenotypes.
Genetic Epidemiology,
35(5), 318-32.
https://doi.org/10.1002/gepi.20580
Pedersen, C. B., Demontis, D.
, Pedersen, M. S., Agerbo, E., Mortensen, P. B., Børglum, A., Hougaard, D.
, Mors, O. & Cantor-Graae, E. (2010).
Can genetic diversity explain the increased risk of schizophrenia among second generation immigrants?. Abstract from 2nd Biennial Schizophrenia International Research Conference, Florence, Italy.
Pedersen, C. B., Demontis, D., Pedersen, M. S., Agerbo, E., Mortensen, P. B., Børglum, A., Hougaard, D. M., Hollegaard, M. V.
, Mors, O. & Cantor-Graae, E. (2012).
Risk of schizophrenia in relation to parental origin and genome-wide divergence.
Psychological Medicine,
42(7), 1515-1521.
https://doi.org/10.1017/S0033291711002376
Pedersen, M. S., Benros, M. E.
, Agerbo, E., Børglum, A. D. & Mortensen, P. B. (2012).
Schizophrenia in patients with atopic disorders with particular emphasis on asthma: A Danish population-based study.
Schizophrenia Research,
138(1), 58-62.
https://doi.org/10.1016/j.schres.2012.02.019
Pedersen, C. B., Bybjerg-Grauholm, J.
, Pedersen, M. G., Grove, J., Agerbo, E., Bækvad-Hansen, M., Poulsen, J. B., Hansen, C. S.
, McGrath, J. J., Als, T. D., Goldstein, J. I., Neale, B. M., Daly, M. J., Hougaard, D. M.
, Mors, O., Nordentoft, M.
, Børglum, A. D., Werge, T.
& Mortensen, P. B. (2018).
The iPSYCH2012 case-cohort sample: new directions for unravelling genetic and environmental architectures of severe mental disorders.
Molecular Psychiatry,
23(1), 6–14.
https://doi.org/10.1038/mp.2017.196
Pedersen, E. M., Agerbo, E., Plana-Ripoll, O., Grove, J., Dreier, J. W., Musliner, K. L., Bækvad-Hansen, M., Athanasiadis, G., Schork, A., Bybjerg-Grauholm, J., Hougaard, D. M., Werge, T., Nordentoft, M.
, Mors, O., Dalsgaard, S., Christensen, J., Børglum, A. D., Mortensen, P. B., McGrath, J. J. ... Vilhjálmsson, B. J. (2022).
Accounting for age of onset and family history improves power in genome-wide association studies.
American Journal of Human Genetics,
109(3), 417-432.
https://doi.org/10.1016/j.ajhg.2022.01.009
Pedersen, E. M., Agerbo, E., Plana-Ripoll, O., Steinbach, J., Krebs, M. D., Hougaard, D. M., Werge, T., Nordentoft, M.
, Børglum, A. D., Musliner, K. L., Ganna, A., Schork, A. J.
, Mortensen, P. B., McGrath, J. J., Privé, F. & Vilhjálmsson, B. J. (2023).
ADuLT: An efficient and robust time-to-event GWAS.
Nature Communications,
14(1), Article 5553.
https://doi.org/10.1038/s41467-023-41210-z
Paternoster, V., Edhager, A. V., Sibbersen, C., Nielsen, A. L., Børglum, A. D., Christensen, J. H. & Palmfeldt, J. (2016).
Quantitative assessment of methyl-esterification and other side reactions in a standard propionylation protocol for detection of histone modifications.
Proteomics.
https://doi.org/10.1002/pmic.201500425
Paternoster, V., Rajkumar, A. P., Nyengaard, J. R., Børglum, A. D., Grove, J. & Christensen, J. H. (2018).
The importance of data structure in statistical analysis of dendritic spine morphology.
Journal of Neuroscience Methods,
296, 93-98.
https://doi.org/10.1016/j.jneumeth.2017.12.022
Paternoster, V., Svanborg, M., Edhager, A. V., Rajkumar, A. P., Eickhardt, E. A., Pallesen, J., Grove, J., Qvist, P., Fryland, T., Wegener, G., Nyengaard, J. R., Mors, O., Palmfeldt, J., Børglum, A. D. & Christensen, J. H. (2019).
Brain proteome changes in female Brd1+/- mice unmask dendritic spine pathology and show enrichment for schizophrenia risk.
Neurobiology of Disease,
124, 479-488.
https://doi.org/10.1016/j.nbd.2018.12.011
Paternoster, V., Edhager, A. V., Qvist, P., Donskov, J. G., Shliaha, P., Jensen, O. N.
, Mors, O., Nielsen, A. L., Børglum, A. D., Palmfeldt, J. & Christensen, J. H. (2021).
Inactivation of the Schizophrenia-associated BRD1 gene in Brain Causes Failure-to-thrive, Seizure Susceptibility and Abnormal Histone H3 Acetylation and N-tail Clipping.
Molecular Neurobiology,
58(9), 4495-4505.
https://doi.org/10.1007/s12035-021-02432-8
Paternoster, V., Cömert, C., Kirk, L. S., la Cour, S. H., Fryland, T., Fernandez-Guerra, P., Stougaard, M., Nyengaard, J. R., Qvist, P., Bross, P., Børglum, A. D. & Christensen, J. H. (2022).
The psychiatric risk gene BRD1 modulates mitochondrial bioenergetics by transcriptional regulation.
Translational Psychiatry,
12(1), Article 319.
https://doi.org/10.1038/s41398-022-02053-2
Paksarian, D.
, Trabjerg, B. B., Merikangas, K. R.
, Mors, O., Børglum, A. D., Hougaard, D. M., McGrath, J. J., Pedersen, C. B., Mortensen, P. B. & Agerbo, E. (2018).
The role of genetic liability in the association of urbanicity at birth and during upbringing with schizophrenia in Denmark.
Psychological Medicine,
48(2), 305-314.
https://doi.org/10.1017/S0033291717001696
Paksarian, D.
, Trabjerg, B. B., Merikangas, K. R.
, Mors, O., Børglum, A. D., Hougaard, D. M., Nordentoft, M., Werge, T.
, Pedersen, C. B., Mortensen, P. B., Agerbo, E. & Horsdal, H. T. (2020).
Adolescent residential mobility, genetic liability and risk of schizophrenia, bipolar disorder and major depression.
British Journal of Psychiatry,
217(1), 390-396.
https://doi.org/10.1192/bjp.2020.8
Østergaard, S. D., Trabjerg, B. B., Als, T. D., Albiñana, C., Privé, F., Vilhjálmsson, B. J., Bækvad-Hansen, M., Bybjerg-Grauholm, J., Hougaard, D. M., Nordentoft, M., Werge, T.
, Demontis, D., Mortensen, P. B., Børglum, A. D., Mors, O. & Agerbo, E. (2020).
Polygenic risk score, psychosocial environment and the risk of attention-deficit/hyperactivity disorder.
Translational Psychiatry,
10(1), Article 335.
https://doi.org/10.1038/s41398-020-01019-6
Olsen, L., Sparsø, T., Weinsheimer, S. M., Dos Santos, M. B. Q.
, Mazin, W., Rosengren, A., Sanchez, X. C., Hoeffding, L. K., Schmock, H., Baekvad-Hansen, M., Bybjerg-Grauholm, J., Daly, M. J., Neale, B. M.
, Pedersen, M. G., Agerbo, E., Mors, O., Børglum, A., Nordentoft, M., Hougaard, D. M. ... Werge, T. (2018).
Prevalence of rearrangements in the 22q11.2 region and population-based risk of neuropsychiatric and developmental disorders in a Danish population: a case-cohort study.
The Lancet Psychiatry,
5(7), 573-580.
https://doi.org/10.1016/S2215-0366(18)30168-8
Nyegaard, M., Quist, P., Groossens, D., Del-Favero, J., Kjeldsen, E., Pedersen, S.
, Zacharov, T. F., Mors, O. & Børglum, A. (2008).
Genomic alterations on chromosome 3p21.1 and 17q21.31 in patients with schizophrenia and controls. Abstract from World Congress on Psychiatric Genetics XV, New York, United States.
Nyegaard, M., Zacharov, T. F., Hedemand, A., Sørensen, K., Nordentoft, M., Nørgaard-Pedersen, B., Werge, T., Andersen, P., Hougaard, D. M.
, Pedersen, C. B., Mortensen, P. B., Mors, O. & Børglum, A. (2008).
Association study between the five subunits of the NMDA receptor (GRIN1, GRIN2A, GRIN2B, GRIN2C and GRIN2D genes) and schizophrenia in a large DAnish sample. Poster session presented at XVIth World Congress on Psychiatric Genetics, Osaka, Japan.
Nyegaard, M., Severinsen, J. E., Als, T. D., Hedemand, A., Straarup, S., Nordentoft, M., McQuillin, A., Bass, N., Lawrence, J., Thirumalai, S., Pereira, A. C. P., Kandaswamy, R., Lydall, G. J., Sklar, P., Scolnick, E., Purcell, S., Curtis, D., Gurling, H. M. D.
, Mortensen, P. B. ... Børglum, A. (2010).
Support of association between BRD1 and both schizophrenia and bipolar affective disorder.
American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics,
153B(2), 582-91.
https://doi.org/10.1002/ajmg.b.31023
Nyegaard, M., Børglum, A. D., Bruun, T. G., Collier, D. A., Russ, C.
, Mors, O., Ewald, H. & Kruse, T. A. (2002).
Novel polymorphisms in the somatostatin receptor 5 (SSTR5) gene associated with bipolar affective disorder.
Molecular Psychiatry,
7(7), 745-54.
https://doi.org/10.1038/sj.mp.4001049
Nyegaard, M., Demontis, D., Foldager, L., Hedemand, A., Flint, T. J., Sørensen, K. M., Andersen, P. S., Nordentoft, M., Werge, T.
, Pedersen, C. B., Hougaard, D. M.
, Mortensen, P. B., Mors, O. & Børglum, A. D. (2010).
CACNA1C (rs1006737) is associated with schizophrenia.
Molecular Psychiatry,
15(2), 119-21.
https://doi.org/10.1038/mp.2009.69
Nyegaard, M., Demontis, D., Thestrup, B. B., Hedemand, A., Sørensen, K. M., Hansen, T., Werge, T., Hougaard, D. M., Yolken, R. H.
, Mortensen, P. B., Mors, O. & Børglum, A. D. (2012).
No association of polymorphisms in human endogenous retrovirus K18 and CD48 with schizophrenia.
Psychiatric Genetics,
22(3), 146-8.
https://doi.org/10.1097/YPG.0b013e328353953c
Nyegaard, M., Overgaard, M. T., Søndergaard, M., Vranas, M., Behr, E. R., Hildebrandt, L., Lund, J., Hedley, P. L., Camm, A. J., Wettrell, G., Fosdal, I., Christiansen, M.
& Børglum, A. D. (2012).
Mutations in calmodulin cause ventricular tachycardia and sudden cardiac death.
American Journal of Human Genetics,
91(4), 703-12.
https://doi.org/10.1016/j.ajhg.2012.08.015
Nyegaard, M., Rendtorff, N. D.
, Nielsen, M. S., Corydon, T. J., Demontis, D., Starnawska, A., Hedemand, A., Buniello, A., Niola, F., Overgaard, M. T., Leal, S. M., Ahmad, W.
, Wikman, F. P., Petersen, K. B., Crüger, D. G., Oostrik, J., Kremer, H., Tommerup, N., Frödin, M.
... Børglum, A. D. (2015).
A Novel Locus Harbouring a Functional CD164 Nonsense Mutation Identified in a Large Danish Family with Nonsyndromic Hearing Impairment.
P L o S Genetics,
11(7), e1005386.
https://doi.org/10.1371/journal.pgen.1005386
Nudel, R., Benros, M. E., Krebs, M. D., Allesøe, R. L., Lemvigh, C. K., Bybjerg-Grauholm, J.
, Børglum, A. D., Daly, M. J., Nordentoft, M.
, Mors, O., Hougaard, D. M.
, Mortensen, P. B., Buil, A., Werge, T., Rasmussen, S. & Thompson, W. K. (2019).
Immunity and mental illness: findings from a Danish population-based immunogenetic study of seven psychiatric and neurodevelopmental disorders.
European Journal of Human Genetics,
27(9), 1445-1455.
https://doi.org/10.1038/s41431-019-0402-9
Nudel, R., Wang, Y., Appadurai, V., Schork, A. J., Buil, A.
, Agerbo, E., Bybjerg-Grauholm, J.
, Børglum, A. D., Daly, M. J.
, Mors, O., Hougaard, D. M.
, Mortensen, P. B., Werge, T., Nordentoft, M., Thompson, W. K. & Benros, M. E. (2019).
A large-scale genomic investigation of susceptibility to infection and its association with mental disorders in the Danish population.
Translational Psychiatry,
9(1), Article 283.
https://doi.org/10.1038/s41398-019-0622-3
Nudel, R., Appadurai, V., Schork, A. J., Buil, A., Bybjerg-Grauholm, J.
, Børglum, A. D., Daly, M. J.
, Mors, O., Hougaard, D. M.
, Mortensen, P. B., Werge, T., Nordentoft, M., Thompson, W. K. & Benros, M. E. (2020).
A large population-based investigation into the genetics of susceptibility to gastrointestinal infections and the link between gastrointestinal infections and mental illness.
Human Genetics,
139(5), 593-604.
https://doi.org/10.1007/s00439-020-02140-8
Nudel, R., Benros, M. E., Krebs, M. D., Allesøe, R. L., Lemvigh, C. K., Bybjerg-Grauholm, J.
, Børglum, A. D., Daly, M. J., Nordentoft, M.
, Mors, O., Hougaard, D. M.
, Mortensen, P. B., Buil, A., Werge, T., Rasmussen, S. & Thompson, W. K. (2021).
Correction: Immunity and mental illness: findings from a Danish population-based immunogenetic study of seven psychiatric and neurodevelopmental disorder (European Journal of Human Genetics, (2019), 27, 9, (1445-1455), 10.1038/s41431-019-0402-9).
European Journal of Human Genetics,
29(8), 1316.
https://doi.org/10.1038/s41431-020-00772-y
Nudel, R., Thompson, W. K.
, Børglum, A. D., Hougaard, D. M.
, Mortensen, P. B., Werge, T., Nordentoft, M. & Benros, M. E. (2022).
Maternal pregnancy-related infections and autism spectrum disorder-the genetic perspective.
Translational Psychiatry,
12, Article 334.
https://doi.org/10.1038/s41398-022-02068-9
Njølstad, P. R., Andreassen, O. A., Brunak, S.
, Børglum, A. D., Dillner, J., Esko, T., Franks, P. W., Freimer, N., Groop, L., Heimer, H., Hougaard, D. M., Hovig, E., Hveem, K., Jalanko, A., Kaprio, J., Knudsen, G. P., Melbye, M., Metspalu, A.
, Mortensen, P. B. ... Stefánsson, K. (2019).
Roadmap for a precision-medicine initiative in the Nordic region.
Nature Genetics,
51(6), 924-930.
https://doi.org/10.1038/s41588-019-0391-1
Nissen, J. B., Søholm Hansen, C.
, Starnawska, A., Mattheisen, M., Børglum, A., Buttenschøn, H. N. & Hollegård, M. (2016).
DNA Methylation at the Neonatal State and at the Time of Diagnosis: Preliminary Support for an Association with the Estrogen Receptor 1, Gamma-Aminobutyric Acid B Receptor 1, and Myelin Oligodendrocyte Glycoprotein in Female Adolescent Patients with OCD.
Frontiers in Psychiatry,
7(35), Article 35.
https://doi.org/10.3389/fpsyt.2016.00035
Nievergelt, C. M., Maihofer, A. X., Klengel, T., Atkinson, E. G., Chen, C. Y., Choi, K. W., Coleman, J. R. I., Dalvie, S., Duncan, L. E., Gelernter, J., Levey, D. F., Logue, M. W., Polimanti, R., Provost, A. C., Ratanatharathorn, A., Stein, M. B., Torres, K., Aiello, A. E., Almli, L. M. ... Koenen, K. C. (2019).
International meta-analysis of PTSD genome-wide association studies identifies sex- and ancestry-specific genetic risk loci.
Nature Communications,
10(1), Article 4558.
https://doi.org/10.1038/s41467-019-12576-w
Nievergelt, C. M., Maihofer, A. X., Atkinson, E. G., Chen, C.-Y., Choi, K. W., Coleman, J. R., Daskalakis, N. P., Duncan, L. E., Polimanti, R., Aaronson, C., Amstadter, A. B.
, Andersen, S. B., Andreassen, O. A., Arbisi, P. A., Ashley-Koch, A. E., Austin, S. B., Avdibegoviç, E., Babic, D., Bacanu, S.-A. ... Koenen, K. C. (2023).
Discovery of 95 PTSD loci provides insight into genetic architecture and neurobiology of trauma and stress-related disorders. medRxiv. medRxiv : the preprint server for health sciences
https://doi.org/10.1101/2023.08.31.23294915
Nicodemus, K. K., Hargreaves, A., Morris, D., Anney, R., Gill, M., Corvin, A., Donohoe, G. & Schizophrenia Psychiatric Genome-wide Association Study (GWAS) Consortium (2014).
Variability in working memory performance explained by epistasis vs polygenic scores in the ZNF804A pathway.
J A M A Psychiatry,
71(7), 778-85.
https://doi.org/10.1001/jamapsychiatry.2014.528
Nexø, B. A., Vogel, U.
, Olsen, A., Nyegaard, M., Bukowy, Z., Rockenbauer, E.
, Zhang, X., Koca, C.
, Mains, M., Hansen, B., Hedemand, A., Kjeldgaard, A. H., Laska, M. J., Raaschou-Nielsen, O., Cold, S.
, Overvad, K., Tjønneland, A.
, Bolund, L. & Børglum, A. (2008).
Linkage disequilibrium mapping of a breast cancer susceptibility locus near RAI/PPP1R13L/iASPP. B M C Medical Genetics,
9(56), 1-12.
https://doi.org/10.1186/1471-2350-9-56
Nexø, B. A., Christensen, T., Frederiksen, J.
, Møller-Larsen, A., Oturai, A. B.
, Villesen, P., Hansen, B., Nissen, K. K., Laska, M. J., Petersen, T. S., Bonnesen, S., Hedemand, A., Wu, T.
, Wang, X., Zhang, X., Brudek, T., Maric, R., Søndergaard, H., Sellebjerg, F. T.
... Pedersen, F. S. (2011).
The Etiology of Multiple Sclerosis: Genetic Evidence for the Involvement of the Human Endogenous Retrovirus HERV-Fc1.
P L o S One,
6(2), e16652.
https://doi.org/10.1371/journal.pone.0016652
Musliner, K. L., Mortensen, P. B., McGrath, J. J., Suppli, N. P., Hougaard, D. M., Bybjerg-Grauholm, J., Bækvad-Hansen, M., Andreassen, O.
, Pedersen, C. B., Pedersen, M. G., Mors, O., Nordentoft, M.
, Børglum, A. D., Werge, T.
, Agerbo, E. & Bipolar Disorder Working Group of the Psychiatric Genomics Consortium (2019).
Association of Polygenic Liabilities for Major Depression, Bipolar Disorder, and Schizophrenia With Risk for Depression in the Danish Population.
JAMA Psychiatry,
76(5), 516-525.
https://doi.org/10.1001/jamapsychiatry.2018.4166
Musliner, K., Vilhjálmsson, B. J., Agerbo, E., Zandi, P. P.
, Mortensen, P. B., Børglum, A. & Østergaard, S. D. (2019).
Polygenic risk and conversion from depression to bipolar disorder. Poster session presented at 32nd ECNP Congress, København, Denmark.
Musliner, K., Mortensen, P. B., McGrath, J. J., Hougaard, D., Baekvad-Hansen, M.
, Pedersen, C. B., Pedersen, M. G., Mors, O., Nordentoft, M.
, Børglum, A., Werge, T., Suppli, N. P.
& Agerbo, E. (2019).
Polygenic liability and depression in the iPSYCH2012 cohort. 1080-1081. Abstract from World Congress of Psychiatric Genetics , Glasgow, United Kingdom.
Musliner, K., Vilhjálmsson, B. J., Albiñana Climent, C., Krebs, M. D., Zandi, P. P.
, Agerbo, E., Mortensen, P. B., Werge, T.
, Børglum, A. & Østergaard, S. D. (2019).
Towards precision medicine in psychiatric care: Using polygenic risk scores to predict outcomes in hospital-treated depression patients . S88-S88. Abstract from World Congress of Psychiatric Genetics , Anaheim , California, United States.
Musliner, K. L., Krebs, M. D.
, Albiñana, C., Vilhjalmsson, B., Agerbo, E., Zandi, P. P., Hougaard, D. M., Nordentoft, M.
, Børglum, A. D., Werge, T.
, Mortensen, P. B. & Østergaard, S. D. (2020).
Polygenic Risk and Progression to Bipolar or Psychotic Disorders Among Individuals Diagnosed With Unipolar Depression in Early Life.
The American Journal of Psychiatry,
177(10), 936-943.
https://doi.org/10.1176/appi.ajp.2020.19111195